@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_head
{
this:
np:hasAssertion
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_assertion
;
np:hasProvenance
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_provenance
;
np:hasPublicationInfo
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_assertion
a
np:Assertion
.
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_provenance
a
np:Provenance
.
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN4cbdec2576f5493470cb78d2d0fc6522
sio:SIO_000628
miriam-gene:2952
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_provenance
{
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_assertion
dcterms:description
"[Our objectives were to compare the frequency of the null genotype for GSTM1, GSTT1, or both in children with ALL to that in healthy controls, and to determine whether GST genotype was associated with treatment outcome and prognostic factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:9057653
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP602137.RAPbsArPwVwO6JG7QtwkeU7LVEcwqFwkEtN4FVV_MKeTE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}